Florence Neal Cooper Smith 5K Walk 4 Sickle Cell

The 2nd annual Florence Neal Cooper Smith 5K Walk 4 Sickle Cell was full of sunshine, hope and high spirits for the future. Photos: Daniel Sangjib Min, MCV Foundation

Highland Springs High School marching band

The Highland Springs High School marching band kicked off the 5K walk. 

Rev. Tyrone Nelson

Rev. Tyrone Nelson, a VCU Health board member and chair of Henrico County Board of Supervisors for the Varina district, shared remarks before the start of the walk. 

Lawrence Cooper

Lawrence Cooper, Florence Neal Cooper Smith’s son, shared remarks as one of the guest speakers. CBS 6 "This Morning" anchor Reba Hollingsworth served as the event’s emcee. 

Florence Neal Cooper Smith

Florence Neal Cooper Smith (seated), founded the Virginia Sickle Cell Anemia Awareness Program on the MCV Campus. 

volunteers

Community events like the Florence Neal Cooper Smith 5K Walk 4 Sickle Cell are not possible without the dedication and commitment of volunteers and hosts like Finding a Cure Together 4 Sickle Cell (F.A.C.T.S.), the Upsilon Omega Chapter of Alpha Kappa Alpha Sorority Inc. and Zenobia's Promise Foundation.

Upsilon Omega Chapter of Alpha Kappa Alpha Sorority Inc.

Members of the Upsilon Omega Chapter of Alpha Kappa Alpha Sorority Inc. with Florence Neal Cooper Smith. Photo: Zaynah Qutubuddin, MCV Foundation

Hope and High Spirits at the 2nd Annual Walk for Sickle Cell

Thanks to the dedication of many Greater Richmond community members, a walk this month raised more than $16,000 for sickle cell disease research, prevention and treatment. 

After a week of mist, clouds and rain, the sun returned, warm and bright for the 2nd annual Florence Neal Cooper Smith 5K Walk 4 Sickle Cell on Sept. 21 at Henrico County’s Dorey Park. 

Sickle cell disease is an inherited blood disease that affects around 100,000 people in the U.S. It causes painful episodes that can be severe and last for days or weeks with serious complications, including stroke, organ damage, acute chest syndrome, and premature death.

malik lawson
Malik Lawson, 19, has lived with sickle cell disease since birth. He is currently a sophomore at Virginia State University studying agriculture. 

Held during Sickle Cell Awareness Month, the event was organized by Finding a Cure Together 4 Sickle Cell (F.A.C.T.S.), with support from the Upsilon Omega Chapter of Alpha Kappa Alpha Sorority Inc. and Zenobia's Promise Foundation. 

“It’s all about the support system around you,” said guest speaker Malik Lawson, a sophomore at Virginia State University who has lived with sickle cell disease since birth. “You all motivate me to keep myself up and keep myself good.”

Last year’s inaugural walk also raised more than $16,000.

All proceeds from the walk benefit the Florence Neal Cooper Smith Professorship at the VCU School of Medicine, which was established in 2014 and is the first of its kind to be named for a Black woman in the U.S. 

florence neal cooper smith and walter davis
Walter Davis, 30 (right), with Florence Neal Cooper Smith. Davis was born with sickle cell disease and was a participant in a newly approved sickle cell gene therapy at the Children’s Hospital of Richmond at VCU and VCU Medical Center, the only qualified treatment centers in the state to offer the therapy. 

Florence Neal Cooper Smith is a Richmond native who has been a tireless advocate for sickle cell awareness and research for more than a half century.

In 1969, she organized Richmond’s first citywide survey to determine awareness of sickle cell disease, and in 1972 she founded the Virginia Sickle Cell Anemia Awareness Program on the MCV Campus with Dr. Robert B. Scott Sr. The program became one of the original 19 federally funded screening clinics in the U.S.

dr. wally smith
Wally R. Smith, M.D. (left), director of VCU Health’s Adult Sickle Cell Program, Del. Delores McQuinn, and Brian Thomas, executive vice president and chief development officer of the MCV Foundation, attended the second annual walk.

Since 1989, an average of 75 newborns in Virginia are diagnosed with sickle cell disease. Thanks to Smith’s efforts, Virginia is a leader in screening all newborn children for sickle cell, and the test is now part of routine newborn screenings. Today, it is estimated that one in 500 African Americans live with the disease, while 1 in 12 are carriers of the sickle cell trait.

The fundraising goal for the Florence Neal Cooper Smith Professorship is $1 million, which, if achieved, would elevate the position to an endowed chair in support of sickle cell research. To date, more than $550,000 has been raised. 

Wally R. Smith, M.D., a nationally recognized expert in sickle cell disease, is the inaugural holder of the professorship and serves as the director of VCU Health’s Adult Sickle Cell Program. He spoke at the event, saying that philanthropically supported research at VCU Health and other academic health systems has already changed and saved lives, and that more community support will continue to help find treatments and ways to cure sickle cell disease. 

sickle cell facts

If you would like to support sickle cell disease research and care on the MCV Campus, please consider making a gift online to the Florence Neal Cooper Smith Professorship by contacting Samantha Charlet, assistant director of development at the MCV Foundation.